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USFDA Consultants Medical Device
Posted by Aniket Chaudhari on July 2, 2024 at 2:30am 0 Comments 0 Likes
Medical Device Manufacturers require USFDA Approvals to sell their products in USA. USFDA differentiates product approvals in Class I, II &III depending upon the risk associated. The submissions include self-certification, 510(k) and PMA depending upon the class of the product.IZiel implements an Outcome-Based Delivery Model to provide complete solution from developing engineering documentation to receiving USFDA Approvals & establishment registrations thereafter. Our teams from USA…
ContinueIQ OQ PQ Medical Devices
Posted by Aniket Chaudhari on July 2, 2024 at 2:29am 0 Comments 0 Likes
IZiel’s Onshore-Offshore Model works with 1 Onsite Member supported by a team of 3-4 engineers from our Technical Center in India. Typically, the data is collected, evaluated and evidence is developed from the process design stage throughout production. Our Model enables the company to complete the project faster and in a cost-effective manner.
Read more@ https://iziel.com/process-validation/
Kitz Ball Valve
Posted by Yusuf Haweliwala on July 2, 2024 at 2:29am 0 Comments 0 Likes
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